Detail
Article
Online article
FT
Medvik - BMC
  • Something wrong with this record ?

Postnatal alteration of monocarboxylate transporter 1 expression in the rat corpus callosum

F. Dong, Y. Liu, Z. Zhang, R. Guo, L. Ma, X. Qu, H. Yu, H. Fan, R. Yao

. 2017 ; 66 (2) : 345-355. [pub] 20161216

Language English Country Czech Republic

Document type Journal Article

In the central nervous system (CNS), monocarboxylate transporter 1 (MCT1) is expressed in astrocytes and endothelial cells but also in oligodendroglia. Oligodendroglia support neurons and axons through lactate transportation by MCT1. Limited information is available on the MCT1 expression changes in candidate cells in the developing rat brain, especially in corpus callosum which is the most vulnerable area in demyelinating diseases. In the present study, we investigated the expression pattern of MCT1 during postnatal development in the rat corpus callosum using immunofluorescene staining, Western blotting analysis and RT-PCR. We reported that MCT1 gene and protein were consistently expressed in the rat corpus callosum from birth to adult. MCT1/CNPase and MCT1/GFAP immunofluorescence staining demonstrated that most of MCT1 positive cells were co-labeled with cyclic nucleotide 3´ phosphodiesterase (CNPase) in rat corpus callosum from P7 to adult, whereas MCT1(+)/GFAP(+) cells preserve the dominate position before P7. Moreover, there were significant associations between the expression of MCT1 protein and the expression of myelin basic protein (MBP) (correlation coefficient: r=0.962, P=0.009) from P7 to adult. Similarly, the MCT1 mRNA expression was also significantly associated with MBP mRNA expression (r=0.976, P=0.005). Our results are proposing that in the developing brain white matter, MCT1 is predominately expressed in oligodendrocyte though it mainly expressed in astrocyte in early postnatal, which indicate that MCT1 may involve in the oligodendrocyte development and myelination.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc18011460
003      
CZ-PrNML
005      
20180502083257.0
007      
ta
008      
180405s2017 xr ad f 000 0|eng||
009      
AR
024    7_
$a 10.33549/physiolres.933365 $2 doi
035    __
$a (PubMed)27982679
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xr
100    1_
$a Dong, Fuxing $u Department of Neurobiology, Xuzhou Medical University, Xuzhou, Jiangsu, People's Republic of China
245    10
$a Postnatal alteration of monocarboxylate transporter 1 expression in the rat corpus callosum / $c F. Dong, Y. Liu, Z. Zhang, R. Guo, L. Ma, X. Qu, H. Yu, H. Fan, R. Yao
520    9_
$a In the central nervous system (CNS), monocarboxylate transporter 1 (MCT1) is expressed in astrocytes and endothelial cells but also in oligodendroglia. Oligodendroglia support neurons and axons through lactate transportation by MCT1. Limited information is available on the MCT1 expression changes in candidate cells in the developing rat brain, especially in corpus callosum which is the most vulnerable area in demyelinating diseases. In the present study, we investigated the expression pattern of MCT1 during postnatal development in the rat corpus callosum using immunofluorescene staining, Western blotting analysis and RT-PCR. We reported that MCT1 gene and protein were consistently expressed in the rat corpus callosum from birth to adult. MCT1/CNPase and MCT1/GFAP immunofluorescence staining demonstrated that most of MCT1 positive cells were co-labeled with cyclic nucleotide 3´ phosphodiesterase (CNPase) in rat corpus callosum from P7 to adult, whereas MCT1(+)/GFAP(+) cells preserve the dominate position before P7. Moreover, there were significant associations between the expression of MCT1 protein and the expression of myelin basic protein (MBP) (correlation coefficient: r=0.962, P=0.009) from P7 to adult. Similarly, the MCT1 mRNA expression was also significantly associated with MBP mRNA expression (r=0.976, P=0.005). Our results are proposing that in the developing brain white matter, MCT1 is predominately expressed in oligodendrocyte though it mainly expressed in astrocyte in early postnatal, which indicate that MCT1 may involve in the oligodendrocyte development and myelination.
650    _2
$a stárnutí $x metabolismus $7 D000375
650    _2
$a zvířata $7 D000818
650    _2
$a novorozená zvířata $7 D000831
650    _2
$a corpus callosum $x metabolismus $7 D003337
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a regulace genové exprese $x fyziologie $7 D005786
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a přenašeče monokarboxylových kyselin $x metabolismus $7 D027501
650    _2
$a orgánová specificita $7 D009928
650    _2
$a krysa rodu Rattus $7 D051381
650    _2
$a potkani Sprague-Dawley $7 D017207
650    _2
$a symportéry $x metabolismus $7 D027981
650    _2
$a tkáňová distribuce $7 D014018
650    _2
$a bílá hmota $x metabolismus $7 D066127
655    _2
$a časopisecké články $7 D016428
700    1_
$a Liu, Yaping $u Laboratory of National Experimental Teaching and Demonstration Center of Basic Medicine, Xuzhou Medical University, Xuzhou, China
700    1_
$a Zhang, Zhenzhong $u Department of Neurobiology, Xuzhou Medical University, Xuzhou, Jiangsu, People's Republic of China
700    1_
$a Guo, Rui $u Department of Neurobiology, Xuzhou Medical University, Xuzhou, Jiangsu, People's Republic of China
700    1_
$a Ma, Li $u Department of Neurobiology, Xuzhou Medical University, Xuzhou, Jiangsu, People's Republic of China
700    1_
$a Qu, Xuebin $u Department of Neurobiology, Xuzhou Medical University, Xuzhou, Jiangsu, People's Republic of China
700    1_
$a Yu, Hongli $u Department of Neurobiology, Xuzhou Medical University, Xuzhou, Jiangsu, People's Republic of China
700    1_
$a Fan, Hongbin $u Department of Neurology, Affiliated Hospital of Xuzhou Medical University, Xuzhou, China
700    1_
$a Yao, Ruiqin $u Department of Neurobiology, Xuzhou Medical University, Xuzhou, Jiangsu, People's Republic of China
773    0_
$w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 66, č. 2 (2017), s. 345-355
856    41
$u https://pubmed.ncbi.nlm.nih.gov/27982679 $y Pubmed
910    __
$a ABA008 $b A 4120 $c 266 $y 4 $z 0
990    __
$a 20180405 $b ABA008
991    __
$a 20180430110107 $b ABA008
999    __
$a ok $b bmc $g 1296239 $s 1008272
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2017 $b 66 $c 2 $d 345-355 $e 20161216 $i 1802-9973 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
LZP    __
$b NLK118 $a Pubmed-20180405

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...